Identity
- Trade Name
- EpiLong Soft Sono FDA UDI
- Generic Name
- Epidural anaesthesia set, non-medicated FDA UDI
- Device Name
- EpiLong Soft Sono FDA UDI
- Model / Reference
- 0631187-51 FDA UDI
- Description
- EpiLong Soft Sono FDA UDI
Identifiers
- Catalog Number
- 0631187-51 FDA UDI
- Primary DI / UDI-DI
- 14048223021535 FDA UDI
- FDA Product Code
- CAZ FDA UDI
- GMDN Term
- Epidural anaesthesia set, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5140 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
EpiLong Soft Sono by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Pajunk GmbH Medizintechnologie
Sources (1)
- FDA UDI 2bef4eec-d182-44b4-b459-38a8062cafe6 36 fields · synced Jun 1, 2026